United States · FDA National Drug Code directory
ACYCLOVIR
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71205-371_32aa3f42-23a1-4867-8228-e6e76cf9f135
- Product NDC
- 71205-371
- Form
- TABLET
- Composition / generic term
- ACYCLOVIR
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130808
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71205-371-30) · 71205-371-30
- 35 TABLET in 1 BOTTLE (71205-371-35) · 71205-371-35
- 60 TABLET in 1 BOTTLE (71205-371-60) · 71205-371-60
- 90 TABLET in 1 BOTTLE (71205-371-90) · 71205-371-90
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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